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BioWorld - Sunday, December 21, 2025
Home » Topics » Drugs » Small molecule

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3D rendering of a molecular glue mediating the interaction between two proteins
Immune

Monte Rosa, Novartis stick together in new $5.7B deal

Sep. 16, 2025
By Lee Landenberger
No Comments
In its second deal with Novartis AG of the past 11 months, Monte Rosa Therapeutics Inc. is getting $120 million up front to collaborate on developing molecular glue degraders to treat immune-mediated diseases. The agreement could swell to $5.7 billion for Monte Rosa.
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3D rendering of a molecular glue mediating the interaction between two proteins

Monte Rosa, Novartis stick together in new $5.7B deal

Sep. 15, 2025
By Lee Landenberger
No Comments
In its second deal with Novartis AG of the past 11 months, Monte Rosa Therapeutics Inc. is getting $120 million up front to collaborate on developing molecular glue degraders to treat immune-mediated diseases. The agreement could swell to $5.7 billion for Monte Rosa.
Read More
Colorized scanning electron micrograph of human respiratory syncytial virus.
Infection

CSPC’s SYH-2066 gains trial clearance in China for RSV

Sep. 15, 2025
No Comments
CSPC Pharmaceutical Group Ltd.’s SYH-2066 tablets has obtained clearance from China’s National Medical Products Administration (NMPA) to enter clinical trials for respiratory infections caused by respiratory syncytial virus (RSV).
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Infection

Merck’s MK-8527 enables long-acting HIV-1 prevention

Sep. 15, 2025
No Comments
Nucleoside reverse transcriptase translocation inhibitors (NRTTIs) are a novel class of antiretroviral agents that inhibit HIV replication by targeting the viral reverse transcriptase enzyme and specifically blocking its translocation step during DNA synthesis, a critical process in the viral replication cycle.
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Intercept’s Ocaliva pulled from US market, placed on clinical hold

Sep. 11, 2025
By Jennifer Boggs
No Comments
When it won U.S. FDA accelerated approval more than eight years ago, Intercept Pharmaceuticals Inc.’s Ocaliva (obeticholic acid) was viewed as a breakthrough, becoming the first new treatment in 20 years for rare, progressive liver disease primary biliary cholangitis (PBC) and, for several years, the only second-line treatment for PBC patients failing to respond to ursodeoxycholic acid. More recently, however, Ocaliva has faced regulatory and safety stumbles, with Intercept now voluntarily pulling the farnesoid X receptor activator from the U.S. market.
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Clinical data illustration

Wall Street solutes phase I data from Maze in CKD, PKU

Sep. 11, 2025
By Randy Osborne
No Comments
Maze Therapeutics Inc. CEO Jason Coloma said the latest phase I results with MZE-782, a prospect for phenylketonuria (PKU) as well as chronic kidney disease (CKD), bolster the firm’s “conviction to move into phase II” next year in both indications.
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Revolution takes early stage cues for a phase III in pancreatic cancer

Sep. 11, 2025
By Lee Landenberger
No Comments
Positive results for Revolution Medicines Inc.’s phase I studies of its lead candidate, the RAS-blocker daraxonrasib for treating pancreatic ductal adenocarcinoma, prompted the company to say it’s time for a phase III study in the aggressive cancer. Revolution said it plans to begin a global, randomized and registrational trial in first-line metastatic disease sometime in the fourth quarter of 2025.
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White tablets spilling out of white bottle, blue background

New guidance offers path for non-opioid drug development

Sep. 10, 2025
By Karen Carey
No Comments
The U.S. FDA issued new guidance for the development of non-opioid analgesics for chronic pain indications, with specific details on trial design, patient populations and meaningful outcomes, including reducing the nation’s reliance on opioids.
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Ovarian cancer illustration

PMV’s rezatapopt wows in ovarian cancer in early phase II readout

Sep. 10, 2025
By Jennifer Boggs
No Comments
PMV Pharmaceuticals Inc.’s rezatapopt yielded impressive overall response data in ovarian cancer, prompting the firm to aim for a potential accelerated approval filing in early 2027. The news caused the firm’s stock (NASDAQ:PMV) to jump in premarket trading, but shares ended the day at $1.27, down 20%, as investors signaled they are clearly holding out for further data confirming broader market potential for the p53-targeting small molecule.
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Digital heart illustration

Braveheart licenses Hengrui's heart drug HRS-1893 in $1B deal

Sep. 9, 2025
By Marian (YoonJee) Chu
No Comments
Braveheart Bio Inc. is paying $65 million up front to license Jiangsu Hengrui Pharmaceuticals Co. Ltd.’s oral hypertrophic cardiomyopathy drug candidate called HRS-1893.
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